| Dr. Gross Interview, S. Carolina |
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Interviewed by Vicky Marlow January 17, 2008
1.) Hi Dr. Gross, can you please first start out by telling us how you got started with Hip Resurfacing and give us a little background on your experience as a surgeon. Where did you train for hip resurfacing? Who trained you? Did you continue your training after starting resurfacing?
I learned to perform hemi-resurfacing during residency; but as many of the current leaders in the field of hip resurfacing, I had to train myself to perform total hip resurfacing 9 years ago. I have performed over 1500 metal-metal resurfacings to date.
2.) Do you do the neck capsule preservation technique in your surgeries?
This is rarely done. I suspect it is very difficult. If I were a patient, I would be hesitant to sign up for this until a surgeon has done over 100 resurfacings this way. Stemmed total hips don’t count; they are much easier to do through any approach.
Dog studies show that the process has already started by 6 weeks postop. I suspect 90% of ultimate strength has developed by 6 months and 100% by 1 year.
If they live within 4 hours of Columbia SC: 1 overnight; discharge about 5pm on the first postoperative day. All others: Discharge noon of postoperative day 2.
I believe they are the future of resurfacing. At this point I am the only US Surgeon with experience using completely uncemented metal-on-metal resurfacings. I hear a lot of doubts and criticism from other surgeons. I’m used to this. I got the same when I started resurfacing 9 years ago. I am confident other surgeons will change their mind and follow my lead eventually. In the last year I have done over 300 fully porous resurfacings. Please see the addendum* if you are interested in reading further on this topic.
My general rules are under 65 age, at least 2/3 of the femoral head viable, and enough socket intact to accept a component without screws. I estimate that almost 40% of all hip replacement patients in the US would qualify. The younger a patient is, the more I bend the other 2 rules to preserve bone stock with resurfacing. I sometimes perform difficult cases with custom implants in young patients.
My comprehensive multimodal pain management program includes spinal anesthetic with a long acting narcotic as well as intravenous sedation. With this program in conjunction with minimally invasive surgery my patients have very little pain during their hospital stay. Most are able to sleep comfortably even the first night after surgery. Most patients are amazed by the lack of any serious pain. The days when patients were miserable with pain after surgery should be long gone. Unfortunately many surgeons have not yet embraced these principles, and their patients suffer needlessly. The only exception to this rule is the group of patients who are addicted to prescription narcotics before surgery. It is difficult to do as good a job with postoperative pain management in this group.
I take on many patients who are higher risk for complication (such as AVN, dysplasia and large cysts) on an individualized basis. Many factors are considered. Small 1-3 cm cysts have not been a problem in my experience.
I do bilateral surgery (only for patients with normal bone strength) on Monday followed by the second surgery on Wednesday. Patients are discharged on Friday at noon.
As the designing surgeon of the BIOMET Recap and Magnum system I have a strong bias towards my own work. I currently prefer the fully porous resurfacing system that I have pioneered. I will implant the hybrid version if a patient prefers.
BIOMET Magnum total hip (large bearing metal-on-metal) with a porous coated stem such as the Mallory. My design. Large bearings are stable, unbreakable and show very high wear resistance. They are the best alternative to Resurfacing.
Surgeon Talent varies tremendously, probably more so than athletic talent. The problem is that it is extremely hard for a non surgeon to evaluate who is best. Some have done large numbers and still are not particularly skilled. Some are good at writing research papers but are not so skilled at cutting. Unless you are a surgeon who knows the literature in this field and can watch several surgeons before they make a decision; I advise you to talk to a few patients who have had a particular surgeon work on them and base most of your decision on this “word of mouth” reputation.
The Birmingham (Smith & Nephew, Richards) total HSR was the first to get FDA approval in the US based on an unprecedented FDA decision to approve this implant on the basis of single (developing) surgeon’s foreign data. Cormet 2000 ( Corin Ltd., Stryker) total HSR was the first to be approved based on the usual mechanism of a US run Multi-center FDA study( approval 7/2007, I was the lead investigator). Therefore, there are now 2 implants available in the US that have an FDA indication for total HSR. |
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